1997
DOI: 10.1097/00005373-199705001-00008
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Hypertonic/Hyperoncotic Saline Attenuates Microcirculatory Disturbances after Traumatic Brain Injury

Abstract: Whether the anti-inflammatory effect of HS/DEX plays a role in reducing delayed brain damage (> 6 hours after TBI) or other systemic complications of TBI arises as an important question and should be investigated further.

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Cited by 100 publications
(31 citation statements)
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“…19,28 Clinically, HTS and mannitol have each been shown, in several observational and nonrandomized studies, to reduce ICP and improve brain physiology to different extents. In an initial prospective study, Härtl et al showed that 7.5% HTS reduced ICP and increased cerebral perfusion pressure (CPP) in patients with TBI.…”
mentioning
confidence: 99%
“…19,28 Clinically, HTS and mannitol have each been shown, in several observational and nonrandomized studies, to reduce ICP and improve brain physiology to different extents. In an initial prospective study, Härtl et al showed that 7.5% HTS reduced ICP and increased cerebral perfusion pressure (CPP) in patients with TBI.…”
mentioning
confidence: 99%
“…38 Using intravital microscopy of pial windows, HTS administration after cerebral percussion injury or systemic thermal injury also reduced EC-PMN interactions. 39,40 Liver intravital microscopy has probably yielded the most exciting findings to date about EC-PMN interactions following the differential fluid resuscitation of hemorrhagic shock. Indeed, several studies report decreases in capillary and sinusoidal luminal narrowing and improved flow parameters, 25,[41][42][43] as well as diminished EC-PMN interactions (sinusoids and postsinusoidal venules) in animals resuscitated with hypertonic fluids.…”
Section: Discussionmentioning
confidence: 99%
“…Furthermore, there is evidence that HS solutions can lead to 1) increased regional perfusion, possibly secondary to dehydration of cerebral endothelial cells and erythrocytes (dehydration of erythrocytes facilitates flow through the capillaries) [12]; 2) increased cardiac output and mean arterial blood pressure (MABP), likely secondary to augmentation of plasma volume and a positive inotropic effect [9••,13••], and the combination of increased MABP and decreased ICP is ideal for increasing cerebral perfusion pressure ([CPP], CPP = MABP -ICP); 3) reduced inflammatory response to brain injury [14]; 4) restoration of normal membrane potentials through normalization of intracellular sodium and chloride concentrations [13]; and 5) improved gas exchange and improved PaO 2 [15] caused by a reduction of extravascular lung volume (Table 1).…”
Section: Mechanism Of Action Of Hypertonic Saline Solutionsmentioning
confidence: 99%